Fast topological imaging

Mathematical optimization methods based on the topological sensitivity analysis have been used to develop innovative ultrasonic imaging methods. With a single illumination of the medium, they have proved experimentally to yield a lateral resolution comparable to classical multiple-illumination techniques. As these methods are based on the numerical simulations of two wave fields, they require extensive computation. A time-domain finite-difference scheme is usually used for that purpose. This paper presents the development of an experimental imaging method based on the topological sensitivity. The numerical cost is reduced by replacing the numerical simulations by simple mathematical operations between the radiation patterns of the array’s transducers and the frequency-domain signals to be emitted. These radiation patterns are preliminary computed once and for all. They were obtained with a finite element model for the anisotropic elastodynamic case and with semi-analytical integrations for the acoustic case. Experimental results are presented for a composite material sample and for a prefractal network immersed in water. A lateral resolution below 2.5 times the wavelength is obtained with a single plane wave illumination. The method is also applied with multiple illuminations, so that objects hidden in complex media can be investigated.     

Isoguanosine derivatives from the Northeastern Atlantic sponge Clathria (Microciona) strepsitoxa

After a chemical screening of subtidal sponges from the Northeastern Atlantic, Clathria (Microciona) strepsitoxa (Poecilosclerida: Microcionidae) was selected for deeper investigation. This first chemical study led to the identification of two new 8-oxoisoguanosine derivatives. The structure elucidation was performed after extensive analyses of spectroscopic (1D and 2D NMR) and HR-ESIMS data and no significant antimicrobial or cytotoxic activity was detected.     

Cracking study of pentakis(dimethylamino)tantalum vapors by Knudsen cell mass spectrometry

Organometallic molecules are commonly used as gaseous precursors in Atomic Layer Deposition/Chemical Vapor Deposition (ALD/CVD) processes. However, the use of these molecules, which are generally thermally unstable at temperatures close to the deposition temperature, requires an understanding of their gas‐phase chemical behavior. The thermal cracking of the gaseous precursor, pentakis(dimethylamino) tantalum (PDMAT), generally adopted in the ALD/CVD TaN deposition processes, has been studied in the temperature range from 343 to 723K using a specific reactor coupled with a high‐temperature mass spectrometer. This reactor – built as tandem Knudsen cells – consists of two superimposed cells. The first stage reactor – an evaporation cell – provides an input saturated vapor flow operating from room temperature to 333K. The second stage cell, named the cracking cell, operated from 333 to 723K in the present study. Experiments showed the appearance of many gaseous species when the cracking temperature increased and, in particular, dimethylamine, corresponding to the saturated organic branches of PDMAT. Decomposition products of the HNC₂H₆ branch were observed at relatively high temperature, namely above 633K. This gas‐phase study – as for the preceding saturated one – shows the presence of oxygen‐containing molecules in PDMAT cracked vapor. Thus, it explains the systematic presence of oxygen contamination in the deposited TaN films observed in ALD/CVD industrial processes. Copyright © 2010 John Wiley & Sons, Ltd.     

A facile synthesis of new β-lactams

Several new β-lactams have been synthesized in good yields, via the cyclization of 3-chloro-N-arylpropionamides in a mixture of N, N-dimethylformamide and anhydrous sodium carbonate under a nitrogen atmosphere.     

Growth kinetic of single and double-walled aluminogermanate imogolite-like nanotubes: an experimental and modeling approach

Atomic Force Microscopy (AFM) and in situ Small Angle X-ray Scattering (SAXS) were used to investigate the evolution of the aluminogermanate imogolite-like nanotubes concentration and morphology during their synthesis. In particular, in situ SAXS allowed quantifying the transformation of protoimogolite into nanotubes. The size distribution of the final nanotubes was also assessed after growth by AFM. A particular attention was focused on the determination of the single and double walled nanotube length distributions. We observed that the two nanotube types do not grow with the same kinetic and that their final length distribution was different. A model of protoimogolites oriented aggregation was constructed to account for the experimental growth kinetic and the length distribution differences.     

Development and validation of a multiplex UHPLC‐MS/MS assay with stable isotopic internal standards for the monitoring of the plasma concentrations of the antiretroviral drugs bictegravir,cabotegravir, doravirine,and rilpivirine in people living with HIV

The widespread use of highly active antiretroviral treatments has dramatically changed the prognosis of people living with HIV (PLWH). However, such treatments have to be taken lifelong raising issues regarding the maintenance of both therapeutic effectiveness and long‐term tolerability. Recently approved or investigational antiretroviral drugs present considerable advantages, allowing once daily oral dosage along with activity against resistant variants (eg, bictegravir and doravirine) and also parenteral intramuscular administration that facilitates treatment adherence (eg, long‐acting injectable formulations such as cabotegravir and rilpivirine). Still, there remains a risk of insufficient or exaggerated circulating exposure due to absorption issues, abnormal elimination, drug‐drug interactions, and others. In this context, a multiplex ultra‐high performance liquid chromatography coupled to tandem mass spectrometry (UHPLC‐MS/MS) bioassay has been developed for the monitoring of plasma levels of bictegravir, cabotegravir, doravirine, and rilpivirine in PLWH. A simple and convenient protein precipitation was performed followed by direct injection of the supernatant into the UHPLC‐MS/MS system. The four analytes were eluted in less than 3 minutes using a reversed‐phase chromatography method coupled with triple quadrupole mass spectrometry detection. This bioassay was fully validated following international guidelines and achieved good performances in terms of trueness (94.7%‐107.5%), repeatability (2.6%‐11%), and intermediate precision (3.0%‐11.2%) over the clinically relevant concentration ranges (from 30 to 9000 ng/mL for bictegravir, cabotegravir, and doravirine and from 10 to 1800 ng/mL for rilpivirine). This sensitive, accurate, and rapid UHPLC‐MS/MS assay is currently applied in our laboratory for routine therapeutic drug monitoring of the oral drugs bictegravir and doravirine and is also intended to be applied for the monitoring of cabotegravir/rilpivirine levels in plasma from PLWH receiving once monthly or every 2‐month intramuscular injection of these long‐acting antiretroviral drugs.     

Coupled experiments and simulations of microstructural damage in wood

In this paper, we explore ways to couple experimental measurements with the numerical simulations of the mechanical properties of wood. For our numerical simulations, we have adopted a lattice approach, where wood fibers or bundles of wood fibers are modeled as discrete structural elements connected by a lattice of spring elements. Element strength and stiffness properties are determined from bulk material properties. Damage is represented by broken lattice elements, which cause both stiffness and strength degradation. The modeling approach was applied to small specimens of spruce subjected to transverse uniaxial tension, and mode I transverse splitting. The model was found to be good at predicting the load-deformation response of both notched and unnotched specimens, including the post-peak softening response. In addition, the damage patterns predicted by the model are consistent with those observed in the experiments.